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Post Market Surveillance Specialist 1

Fresenius Medical Care North America

Reynosa

Presencial

MXN 923,000 - 1,293,000

Jornada completa

Hace 30+ días

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Descripción de la vacante

A leading healthcare company in Reynosa, Tamaulipas is seeking a Post Market Surveillance Specialist to handle product inquiries and complaints. The ideal candidate will have a Bachelor's degree in a healthcare-related field and 2-5 years of relevant experience in the healthcare/device industry. Strong interpersonal skills and bilingual proficiency in English and Spanish are required. This position involves working closely with customers and various internal departments to ensure compliance and quality standards.

Formación

  • 2 – 5 years of related experience in healthcare/device industry preferred.
  • Understanding of drug/device safety requirements is preferred.
  • Prior experience processing medical device or drug complaints preferred.

Responsabilidades

  • Develops professional expertise and resolves issues following company policies.
  • Interfaces with Customer Service and customers/patients for complaint handling.
  • Enters data into the Complaint Management Database as per good documentation practices.

Conocimientos

Interpersonal skills
PC computer skills
Knowledge of complaint management systems
Familiarity with medical terminology
Bilingual (English/Spanish)

Educación

Bachelor's degree in healthcare related field

Herramientas

MS Access
Excel
Crystal reporting
Descripción del empleo

Post Market Surveillance Specialist

Responsibilities:
  • Developing professional expertise, applies company policies and procedures to resolve a variety of issues.
  • Interfaces with Customer Service and customers/patients to gather additional information required for complaint initiation/investigations, including the retrieval of product samples and or durable equipment retrieval for evaluation.
  • Ensures that complaints from multiple sources (i.e. email, phone, verbal, fax, etc.) are entered into the complaint database.
  • Responsible for receiving, reviewing, and entering data into the Compliant Management Database regarding customer/patient product inquiries and complaints using good documentation practices (GDP).
  • Works on problems of moderate scope where analysis of situation or data requires a review of a variety of factors. Exercises judgment within defined procedures and practices to determine appropriate action.
  • Ensures that durable Equipment CRM Technical Service reports are correctly identified as to status for transfer into system.
  • Determines product and incident complaint codes based on the master symptom code severity list.
  • Notifies customer of receipt of product inquiry/complaint and provides preliminary support as required.
  • Prepares other customer communication (response letters, acknowledgement letters) as appropriate.
  • Partners with sales, marketing, and manufacturing departments to resolve product problems and provides feedback to customers as needed.
  • Assists with review of the timely coding of completed investigations, closure of all complaint files, and ensures that all pertinent information is contained consistently and uniformly within the file prior to closure.
  • Performs queries to provide complaint data and ad hoc trend analysis on reported product problems/complaints.
  • Interfaces with Corporate Quality Engineering and the RTG manufacturing sites as required for product investigations/trends.
  • Adheres to the FMCNA Compliance Program, including following all regulatory and division/company policy requirements.
  • Strives to meet Accuracy Goals (95% accuracy goal). Ensures data is collected through routine business
Qualifications:
  • Bachelor's degree preferred, preferably in a healthcare related field.
  • Minimum 2 – 5 years of related experience in the healthcare/device industry or exposure to medical device quality system regulations; understanding of drug/device safety requirements are preferred; with an Advanced Degree no prior experience may be considered.
  • Prior experience processing medical device or drug complaints preferred.
  • Strong interpersonal skills.
  • Knowledge based PC computer skills essential, such as industry recognized complaint management systems, crystal reporting, MS Access and Excel.
  • Familiarity with medical terminology is preferred.
  • Bilingual (English/Spanish) Fluent in English.
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